Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Junsu Yang"'
Autor:
Bentuo Zhang, Qiang Gang, Lingchao Meng, Zhenyu Li, Xujun Chu, Haohao Wu, Junsu Yang, Baogang Huang, Kang Du
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-7 (2024)
Abstract Distal hereditary motor neuropathies (dHMN) are a group of heterogeneous diseases and previous studies have reported that the compound heterozygous recessive MME variants cause dHMN. Our study found a novel homozygous MME variant and a repor
Externí odkaz:
https://doaj.org/article/a59a221d562c413cbf2e529d47a4d533
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
This study reported a case of MELAS syndrome presenting as the initial imaging characteristics of Fahr’s syndrome with “near” sudden unexpected death in epilepsy (SUDEP) and lateralized periodic discharges (LPD). The patient, a young boy, exper
Externí odkaz:
https://doaj.org/article/4e7c7dba2ea74759b291f9f85ea96a43
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
ObjectiveThe over-age phenomenon of simple febrile seizures (SFS) was found during the epidemic in COVID-19, but there was no clear explanation, especially in China. This study aimed to analyze the clinical and auxiliary examination features of SFS i
Externí odkaz:
https://doaj.org/article/3dbd6887a36e4764a2fec2e45836f601
Publikováno v:
Journal of Healthcare Engineering.
Objectives. Epilepsy is a chronic neurological disorder that is characterized by episodes of seizure. Methods. In this study, patients with status epilepticus in the Intensive Care Unit of the Department of Neurology of Qujing First People’s Hospit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d718169ee7a4b26bf71dc8e2e91fe36c
Autor:
Junsu Yang, Dong Yang, Xuefeng Guang, Qiang Xue, Xiang Ma, Hongwen Zhu, Ruiqiong Ba, Li Zhang, Yi-Bing Lu, Weihua Zhang
Publikováno v:
Journal of Thrombosis and Thrombolysis. 42:610-615
The expression of let-7 family members was differentiated in ischemic stroke (IS), functioning as an important regulating molecular in the pathophysiology of stroke. We hypothesized that genetic polymorphism in the promoters of let-7 family may be as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b7368b5fb5c13b0418de19e8c55827e
https://doi.org/10.1007/s11239-016-1400-1
https://doi.org/10.1007/s11239-016-1400-1
Publikováno v:
Medicine; 12/24/2020, Vol. 99 Issue 52, p1-5, 5p